产品中心 流式试剂&相关 流式抗体

所有图片(1/1)

Alexa Fluor® 647 Rat Anti-Mouse Ki67 Antibody (S-R595)

Proliferation marker protein Ki-67,Antigen identified by monoclonal antibody Ki-67 homolog (Antigen KI-67 homolog,Antigen Ki67 homolog),Mki67

价格 1,150.00 供应商现货 : 3-5个工作日
货号 S0B5499
规格
数量
收藏 分享

产品介绍 评论(0)

产品规格
  • 宿主来源

    Rat
  • 抗原名称

    Ki67
  • 分子别名

    Proliferation marker protein Ki-67; Antigen identified by monoclonal antibody Ki-67 homolog (Antigen KI-67 homolog; Antigen Ki67 homolog); Mki67
  • 细胞定位

    Nucleus
  • Accession

    E9PVX6
  • 克隆号

    S-R595
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2a,k
  • 反应种属 ?

    Ms
  • 阳性样本

    NIH/3T3
  • 纯化方式

    Protein G
  • 浓度

    0.05mg/ml
  • 标记

    Alexa Fluor® 647
  • 性状

    Liquid
  • 缓冲体系

    PBS, 1% BSA, 0.3% Proclin 300
  • 储存条件

    12 months from date of receipt / reconstitution, 2 to 8 °C as supplied.
  • 应用

    ICFCM

  • 稀释度

    应用 稀释度 推荐种属
    ICFCM 5μl per million cells in 100μl volume Ms
背景介绍
  • Ki67 protein is a non-histone nuclear protein encoded by the MKI67 gene, widely used as a proliferation marker in pathology. It is expressed during all active phases of the cell cycle—G1, S, G2, and M—but is absent in quiescent (G0) cells. Ki67 has multiple molecular functions, including forming the perichromosomal layer to prevent chromosome aggregation during mitosis and organizing heterochromatin. It also facilitates chromosome attachment to the mitotic spindle and individual chromosome mobility. In addition to its role in cell division, Ki67 is a valuable prognostic and predictive indicator in cancer diagnosis, with its expression levels correlating with tumor cell proliferation rates.

  • 流式分析

    • Flow cytometric analysis of Mouse Ki67 expression on proliferating NIH/3T3 cells. Cells from the NIH/3T3 (Mouse embryonic fibroblast) was stained with either Alexa Fluor® 647 Rat IgG2a, κ Isotype Control (Black line histogram) or SDT Alexa Fluor® 647 Rat Anti-Mouse Ki67 Antibody (Red line histogram) at 5 μl/test, cells without incubation with primary antibody and secondary antibody (Blue line histogram) was used as unlabelled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

评论(0)